Phenotype #0000039464

Individual ID 00052887
Associated disease LCA
Phenotype details Leber congenital amaurosis; macular degeneration, absence of normal pupil response, pigmentary changes over time, poor or loss in night vision, nystagmus, severe rod-cone dystrophy, night blindness
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Muhammad Ajmal
Database submission license No license selected
Created by Muhammad Ajmal